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NDC 00642-0079-12 Vitafol OB 30; 70; 100; 2; 12; 1; 65; 25; 18; 2.5; 1.8; 1.6; 2700; 400; 25 [iU]/1; mg/1; mg/1; mg/1; ug/1; mg/1; mg/1; mg/1; mg/1; mg/1; mg/1; mg/1; [iU]/1; [iU]/1; mg/1 Details
Vitafol OB 30; 70; 100; 2; 12; 1; 65; 25; 18; 2.5; 1.8; 1.6; 2700; 400; 25 [iU]/1; mg/1; mg/1; mg/1; ug/1; mg/1; mg/1; mg/1; mg/1; mg/1; mg/1; mg/1; [iU]/1; [iU]/1; mg/1
Vitafol OB is a ORAL TABLET in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by Exeltis USA, Inc.. The primary component is .ALPHA.-TOCOPHEROL; ASCORBIC ACID; CALCIUM; COPPER; CYANOCOBALAMIN; FOLIC ACID; IRON; MAGNESIUM; NIACIN; PYRIDOXINE HYDROCHLORIDE; RIBOFLAVIN; THIAMINE MONONITRATE; VITAMIN A; VITAMIN D; ZINC.
Product Information
| NDC | 00642-0079 |
|---|---|
| Product ID | 0642-0079_f12aec60-46b4-6b23-e053-2995a90acb08 |
| Associated GPIs | 78512015000366 |
| GCN Sequence Number | 061839 |
| GCN Sequence Number Description | prenatal vit 10/iron fum/folic TABLET 65 MG-1 MG ORAL |
| HIC3 | C6F |
| HIC3 Description | PRENATAL VITAMIN PREPARATIONS |
| GCN | 97624 |
| HICL Sequence Number | 034255 |
| HICL Sequence Number Description | PRENATAL VITS WITH CALCIUM NO.10/FERROUS FUMARATE/FOLIC ACID |
| Brand/Generic | Brand |
| Proprietary Name | Vitafol OB |
| Proprietary Name Suffix | Caplet |
| Non-Proprietary Name | Vitamin A, Ascorbic Acid, Vitamin D, .Alpha.-Tocopherol, Thiamine Mononitrate, Riboflavin, Niacin, Pyridoxine Hydrochloride, Folic Acid, Cyanocobalamin, Calcium, Iron, Magnesium, Zinc, and Copper |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Dosage Form | TABLET |
| Route | ORAL |
| Active Ingredient Strength | 30; 70; 100; 2; 12; 1; 65; 25; 18; 2.5; 1.8; 1.6; 2700; 400; 25 |
| Active Ingredient Units | [iU]/1; mg/1; mg/1; mg/1; ug/1; mg/1; mg/1; mg/1; mg/1; mg/1; mg/1; mg/1; [iU]/1; [iU]/1; mg/1 |
| Substance Name | .ALPHA.-TOCOPHEROL; ASCORBIC ACID; CALCIUM; COPPER; CYANOCOBALAMIN; FOLIC ACID; IRON; MAGNESIUM; NIACIN; PYRIDOXINE HYDROCHLORIDE; RIBOFLAVIN; THIAMINE MONONITRATE; VITAMIN A; VITAMIN D; ZINC |
| Labeler Name | Exeltis USA, Inc. |
| Pharmaceutical Class | Analogs/Derivatives [Chemical/Ingredient], Ascorbic Acid [CS], Calcium [CS], Calcium [EPC], Copper [CS], Copper-containing Intrauterine Device [EPC], Decreased Embryonic Implantation [PE], Decreased Sperm Motility [PE], Inhibit Ovum Fertilization [PE], Ni |
| DEA Schedule | n/a |
| Marketing Category | UNAPPROVED DRUG OTHER |
| Application Number | n/a |
| Listing Certified Through | 2024-12-31 |
Package
NDC 00642-0079-12 (00642007912)
| NDC Package Code | 0642-0079-12 |
|---|---|
| Billing NDC | 00642007912 |
| Package | 100 TABLET in 1 CARTON (0642-0079-12) |
| Marketing Start Date | 2002-12-02 |
| NDC Exclude Flag | N |
| Pricing Information | N/A |